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Takeda Receives Positive CHMP Opinion for Fruquintinib in Previously Treated Metastatic Colorectal Cancer

− If Approved in the European Union, Fruquintinib Will Be the First Novel Targeted Therapy for Metastatic Colorectal Cancer Regardless of Biomarker Status in Over a Decade − Positive Opinion.

Al qahirahUnited statesHong kongAhcene djaballahGastroenterol hepatolAwny farajallahTakeda pharmaceuticalsDrug administrationEuropean commissionJapan pharmaceuticalsExchange commissionEuropean medicines agencyAmerican cancer societyInternational agency for research on cancerInternational normalized ratioCommittee for medicinal products human use

Hutchmed notes CHMP s positive opinion for fruiquintinib approval

Hutchmed notes CHMP s positive opinion for fruiquintinib approval
lse.co.uk - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from lse.co.uk Daily Mail and Mail on Sunday newspapers.

Hong kongAwny farajallahTakeda pharmaceutical co ltdAlliance news ltdEuropean commissionEuropean unionAlliance newsHutchmed china ltd onMedicinal productsHuman useEuropean medicines agencyTakeda chief medical officer awnySabrina pentyAll rights

Takeda to Present Data at 65th American Society of Hematology (ASH) Annual Meeting, Demonstrating Continued Commitment to Patients with Hematologic Diseases

Company to Feature 17 Company-Sponsored and Nine Collaborative Abstracts in Oncology and Hematology Hematology Presentations Include New Data from the Phase 3 and Continuation Trials Supporting.

San diegoUnited statesJohn cunninghamAwny farajallahGerman hodgkin study groupEuropean unionTakeda pharmaceutical company limitedTakeda pharmaceuticalsHealth canadaDrug administrationTakeda pharmaceuticals united statesa incExchange commissionImportant safety information european unionJapan ministry of healthEuropean medicines agencyTakeda pharmaceuticals international

Takeda announces EC approval for Adcetris combination in Hodgkin lymphoma

Takeda announces EC approval for Adcetris combination in Hodgkin lymphoma
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Brentuximab Vedotin Plus AVD Wins EU Approval for Previously Untreated CD30+ Stage III Hodgkin Lymphoma

The European Commission has approved brentuximab vedotin in combination with doxorubicin, vinblastine, and dacarbazine for the treatment of adult patients with previously untreated, CD30-positive, stage III Hodgkin lymphoma.

Awny farajallahBrentuximab vedotinWorld health organizationEuropean commissionEuropean medicine agencyMedicinal productsHuman useAnn arborHematologic oncologyGlobal oncologyy